Variant report

Variant	nsv584014
Chromosome Location	chr2:186293335-186422662
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:404)
CpG islands
(count:244)
Chromatin interactive
region (count:17)
LncRNA
region (count:20)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:404 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr2:186340618-186340908	H1-hESC	embryonic stem cell:	n/a	n/a
2	BATF	chr2:186404043-186404204	GM12878	blood:	n/a	chr2:186404092-186404101
3	BCL3	chr2:186338970-186339324	GM12878	blood:	n/a	n/a
4	CBX3	chr2:186321328-186321586	HCT-116	colon:	n/a	n/a
5	CCNT2	chr2:186421366-186421432	K562	blood:	n/a	n/a
6	CEBPB	chr2:186355813-186356061	HepG2	liver:	n/a	chr2:186355919-186355932 chr2:186355919-186355930
7	CEBPB	chr2:186313713-186313937	HepG2	liver:	n/a	chr2:186313826-186313837 chr2:186313826-186313839
8	CEBPB	chr2:186414165-186414407	IMR90	lung:	n/a	chr2:186414287-186414298
9	CEBPB	chr2:186328234-186328579	HepG2	liver:	n/a	chr2:186328405-186328416
10	CEBPB	chr2:186326049-186326249	HepG2	liver:	n/a	chr2:186326152-186326163
11	CEBPB	chr2:186414148-186414425	HepG2	liver:	n/a	chr2:186414287-186414298
12	CEBPB	chr2:186364789-186365076	HepG2	liver:	n/a	chr2:186364927-186364940 chr2:186364928-186364939 chr2:186364879-186364891
13	CEBPB	chr2:186338338-186338358	HepG2	liver:	n/a	n/a
14	CEBPB	chr2:186321229-186321715	HCT-116	colon:	n/a	n/a
15	CEBPB	chr2:186330125-186330406	HepG2	liver:	n/a	chr2:186330266-186330277
16	CEBPB	chr2:186300444-186300644	H1-hESC	embryonic stem cell:	n/a	chr2:186300612-186300623
17	CEBPB	chr2:186296703-186297026	IMR90	lung:	n/a	n/a
18	CEBPB	chr2:186412355-186412597	HepG2	liver:	n/a	n/a
19	CEBPB	chr2:186301535-186301733	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr2:186296738-186297007	A549	lung:	n/a	n/a
21	CEBPB	chr2:186328274-186328568	A549	lung:	n/a	chr2:186328405-186328416
22	CEBPB	chr2:186414221-186414307	H1-hESC	embryonic stem cell:	n/a	chr2:186414287-186414298
23	CEBPB	chr2:186301521-186301830	HepG2	liver:	n/a	n/a
24	CEBPB	chr2:186326140-186326258	A549	lung:	n/a	chr2:186326152-186326163
25	CEBPB	chr2:186389223-186389330	HepG2	liver:	n/a	chr2:186389247-186389258
26	CEBPB	chr2:186367300-186367396	HepG2	liver:	n/a	n/a
27	CEBPB	chr2:186319765-186320025	HepG2	liver:	n/a	chr2:186319845-186319856 chr2:186319872-186319885 chr2:186319845-186319858
28	CEBPB	chr2:186300587-186300787	HepG2	liver:	n/a	chr2:186300612-186300623
29	CEBPB	chr2:186296748-186297009	HepG2	liver:	n/a	n/a
30	CHD2	chr2:186349402-186349696	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTCF	chr2:186394220-186394370	HFF-Myc	foreskin:	n/a	n/a
32	CTCF	chr2:186387260-186387410	SK-N-SH_RA	brain:	n/a	n/a
33	CTCF	chr2:186340600-186340750	RPTEC	kidney:	n/a	n/a
34	CTCF	chr2:186387331-186387451	HUVEC	blood vessel:	n/a	n/a
35	CTCF	chr2:186340640-186340790	HBMEC	blood vessel:	n/a	n/a
36	CTCF	chr2:186340680-186340830	HAc	cerebellar:	n/a	n/a
37	CTCF	chr2:186387260-186387410	GM06990	blood:	n/a	n/a
38	CTCF	chr2:186387340-186387490	GM12864	blood:	n/a	n/a
39	CTCF	chr2:186306360-186306510	HCT-116	colon:	n/a	chr2:186306416-186306424 chr2:186306417-186306425
40	CTCF	chr2:186340680-186340830	BE2_C	brain:	n/a	n/a
41	CTCF	chr2:186387187-186387605	MCF-7	breast:	n/a	n/a
42	CTCF	chr2:186387319-186387493	MCF-7	breast:	n/a	n/a
43	CTCF	chr2:186388999-186389045	LNCaP	prostate:	n/a	n/a
44	CTCF	chr2:186340680-186340830	HMEC	breast:	n/a	n/a
45	CTCF	chr2:186359746-186359802	GM20000	blood:	n/a	n/a
46	CTCF	chr2:186340640-186340790	MCF-7	breast:	n/a	n/a
47	CTCF	chr2:186387280-186387430	HEEpiC	esophagus:	n/a	n/a
48	CTCF	chr2:186387272-186387522	MCF-7	breast:	n/a	n/a
49	CTCF	chr2:186331000-186331150	HRPEpiC	eye:	n/a	n/a
50	CTCF	chr2:186387351-186387423	K562	blood:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:186412305-186412355	HCPEpiC	choroid plexus:	n/a
2	chr2:186412612-186412662	SK-N-SH	brain:	n/a
3	chr2:186412305-186412355	LNCaP	prostate:	n/a
4	chr2:186412612-186412662	AoSMC	blood vessel:	n/a
5	chr2:186412305-186412355	AG10803	skin:	n/a
6	chr2:186412305-186412355	BJ	skin:	n/a
7	chr2:186412305-186412355	HCT-116	colon:	n/a
8	chr2:186412612-186412662	LNCaP	prostate:	n/a
9	chr2:186412073-186412123	LNCaP	prostate:	n/a
10	chr2:186412305-186412355	BE2_C	brain:	n/a
11	chr2:186412073-186412123	GM12892	blood:	n/a
12	chr2:186412305-186412355	HNPCEpiC	eye:	n/a
13	chr2:186295841-186295891	HCT-116	colon:	n/a
14	chr2:186412612-186412662	HCM	heart:	n/a
15	chr2:186412305-186412355	HIPEpiC	eye:	n/a
16	chr2:186412073-186412123	K562	blood:	n/a
17	chr2:186412305-186412355	SAEC	small airway:	n/a
18	chr2:186412073-186412123	AG10803	skin:	n/a
19	chr2:186412305-186412355	HEEpiC	esophagus:	n/a
20	chr2:186412305-186412355	Jurkat	blood:	n/a
21	chr2:186412612-186412662	GM12892	blood:	n/a
22	chr2:186295841-186295891	AG04449	skin:	fetal
23	chr2:186412305-186412355	GM19239	blood:	n/a
24	chr2:186412073-186412123	HL-60	blood:	n/a
25	chr2:186412612-186412662	NT2-D1	testis:	n/a
26	chr2:186295841-186295891	LNCaP	prostate:	n/a
27	chr2:186412073-186412123	PFSK-1	brain:	n/a
28	chr2:186412612-186412662	RPTEC	kidney:	n/a
29	chr2:186412612-186412662	HRCEpiC	kidney:	n/a
30	chr2:186295841-186295891	SK-N-MC	brain:	n/a
31	chr2:186412612-186412662	HepG2	liver:	n/a
32	chr2:186412612-186412662	GM12891	blood:	n/a
33	chr2:186412073-186412123	HCF	heart:	n/a
34	chr2:186412305-186412355	Hepatocyte	liver:	n/a
35	chr2:186295841-186295891	NB4	blood:	n/a
36	chr2:186412305-186412355	GM06990	blood:	n/a
37	chr2:186412305-186412355	SK-N-MC	brain:	n/a
38	chr2:186412305-186412355	HUVEC	blood vessel:	n/a
39	chr2:186412612-186412662	BJ	skin:	n/a
40	chr2:186295841-186295891	HIPEpiC	eye:	n/a
41	chr2:186412073-186412123	GM12891	blood:	n/a
42	chr2:186295841-186295891	ProgFib	skin:	n/a
43	chr2:186412073-186412123	AG09309	skin:	n/a
44	chr2:186412073-186412123	HIPEpiC	eye:	n/a
45	chr2:186295841-186295891	GM12892	blood:	n/a
46	chr2:186412305-186412355	T-47D	breast:	n/a
47	chr2:186295841-186295891	RPTEC	kidney:	n/a
48	chr2:186412305-186412355	GM12891	blood:	n/a
49	chr2:186412305-186412355	AG04449	skin:	fetal
50	chr2:186295841-186295891	NHDF-neo	bronchial:	n/a

(count:17 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:186378260..186381061-chr2:186398766..186401353,2	K562	blood:
2	chr2:186357997..186360182-chr2:186363444..186366189,2	MCF-7	breast:
3	chr2:186361713..186363240-chr2:186364874..186366648,2	K562	blood:
4	chr2:186334605..186336794-chr2:186340639..186343119,2	MCF-7	breast:
5	chr2:186414202..186416307-chr2:186419424..186421288,2	K562	blood:
6	chr2:186359864..186363240-chr2:186363578..186366648,4	K562	blood:
7	chr2:186361713..186363240-chr2:186364874..186366648,2	K562	blood:
8	chr2:186357997..186360182-chr2:186363444..186366189,2	MCF-7	breast:
9	chr1:174445047..174445587-chr2:186343137..186343750,2	MCF-7	breast:
10	chr2:186291344..186293651-chr2:186297486..186299914,2	K562	blood:
11	chr15:50184826..50185646-chr2:186340212..186341106,2	MCF-7	breast:
12	chr2:186414202..186416307-chr2:186419424..186421288,2	K562	blood:
13	chr2:186359864..186363240-chr2:186363578..186366648,4	K562	blood:
14	chr2:186334605..186336794-chr2:186340639..186343119,2	MCF-7	breast:
15	chr2:186378260..186381061-chr2:186398766..186401353,2	K562	blood:
16	chr2:186387075..186388294-chr2:186603348..186604298,5	MCF-7	breast:
17	chr2:186291344..186293651-chr2:186297486..186299914,2	K562	blood:

(count:20 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZSWIM2-15	chr2:186292850-186293692	ucscGeneNc_uc002upi_2
2	lnc-FSIP2-5	chr2:186370427-186370468	NONHSAT075962
3	lnc-FSIP2-5	chr2:186370211-186370365	NONHSAT075962
4	lnc-ZSWIM2-15	chr2:186302301-186302409	ucscGeneNc_uc002upi_2
5	lnc-FSIP2-5	chr2:186408484-186409210	NONHSAT075962
6	lnc-FSIP2-5	chr2:186403858-186404073	NONHSAT075962
7	lnc-FSIP2-5	chr2:186366772-186369632	NONHSAT075963
8	lnc-FSIP2-5	chr2:186410628-186411001	NONHSAT075962
9	lnc-FSIP2-5	chr2:186369880-186375991	NONHSAT075963
10	lnc-FSIP2-5	chr2:186410448-186410599	NONHSAT075962
11	lnc-FSIP2-5	chr2:186327396-186327672	NONHSAT075962
12	lnc-FSIP2-5	chr2:186347761-186347818	NONHSAT075962
13	lnc-FSIP2-5	chr2:186411283-186411299	NONHSAT075962
14	lnc-ZSWIM2-15	chr2:186309034-186309104	ucscGeneNc_uc002upi_2
15	lnc-FSIP2-5	chr2:186298824-186298920	NONHSAT075962
16	lnc-FSIP2-5	chr2:186369727-186370202	NONHSAT075962
17	lnc-ZSWIM2-15	chr2:186311542-186311686	ucscGeneNc_uc002upi_2
18	lnc-FSIP2-5	chr2:186371629-186371957	NONHSAT075962
19	lnc-FSIP2-5	chr2:186411316-186411619	NONHSAT075962
20	lnc-FSIP2-5	chr2:186386989-186387497	NONHSAT075962

No data

Variant related genes	Relation type
ENSG00000225406	TF binding region
ENSG00000225406	CpG island
ENSG00000188738	chromatin interactions
ENSG00000226747	chromatin interactions

Extended variants
information (count: 4758 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:4758 , 50 per page) page: 1 2 3 4 5 6 7 ... 96

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs13036091	chr2:186293335-186293336	Weak transcription Active TSS	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs190608887	chr2:186293340-186293341	Weak transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
3	rs531889478	chr2:186293349-186293350	Weak transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
4	rs548503824	chr2:186293366-186293367	Weak transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
5	rs144488780	chr2:186293373-186293374	Weak transcription Active TSS	lncRNA	n/a	Overlapped CNVs	n/a
6	rs35815004	chr2:186293415-186293416	Weak transcription ZNF genes & repeats	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs529464631	chr2:186293428-186293429	Weak transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
8	rs145414784	chr2:186293448-186293449	Weak transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
9	rs183593960	chr2:186293453-186293454	Weak transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
10	rs372103445	chr2:186293455-186293456	Weak transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
11	rs537696491	chr2:186293457-186293458	Weak transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
12	rs534139158	chr2:186293473-186293474	Weak transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
13	rs566499122	chr2:186293500-186293501	Weak transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
14	rs533838365	chr2:186293512-186293513	Weak transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
15	rs115634606	chr2:186293534-186293535	Weak transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
16	rs566411856	chr2:186293551-186293552	Weak transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
17	rs573853994	chr2:186293556-186293557	Weak transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
18	rs537995992	chr2:186293595-186293596	Weak transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
19	rs556405877	chr2:186293597-186293598	Weak transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
20	rs17403617	chr2:186293599-186293600	Weak transcription ZNF genes & repeats	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs187817564	chr2:186293609-186293610	Weak transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
22	rs192785899	chr2:186293645-186293646	Weak transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
23	rs572451415	chr2:186293710-186293711	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs377105997	chr2:186293714-186293715	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs149183361	chr2:186293749-186293750	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs184415638	chr2:186293751-186293752	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs531928003	chr2:186293764-186293765	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs549937580	chr2:186293788-186293789	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs67992386	chr2:186293851-186293852	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs532850765	chr2:186293892-186293893	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs374970735	chr2:186293910-186293911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs187760263	chr2:186293913-186293914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs551102936	chr2:186293943-186293944	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs111631200	chr2:186293957-186293958	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs6735605	chr2:186293980-186293981	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs548708674	chr2:186293989-186293990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs567514175	chr2:186294048-186294049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs200014614	chr2:186294079-186294080	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs35504999	chr2:186294086-186294087	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs192714298	chr2:186294090-186294091	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs144811624	chr2:186294091-186294092	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs375468510	chr2:186294113-186294114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs184847406	chr2:186294133-186294134	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs62198857	chr2:186294155-186294156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs17331724	chr2:186294167-186294168	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs539123565	chr2:186294168-186294169	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs147997642	chr2:186294184-186294185	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs372254996	chr2:186294197-186294198	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs554386692	chr2:186294211-186294212	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs148506025	chr2:186294307-186294308	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:55)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	18522746	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	16272173	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
Colorectal cancer	16272173	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Glioblastoma	21080181	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Facial dysmorphism	20548289	CNVD
Mental retardation	20548289	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Sudden cardiac death	19188705	CNVD
Autism	19329560	CNVD
Autism	22543975	CNVD
Urothelial carcinoma	21177765	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:331 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:186291000-186295600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr2:186291200-186297800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr2:186292000-186296600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr2:186292000-186297800	Weak transcription	H9 Cell Line	embryonic stem cell
5	chr2:186292000-186297800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr2:186292000-186298000	Weak transcription	HUES48 Cell Line	embryonic stem cell
7	chr2:186292000-186298200	Weak transcription	H1 Cell Line	embryonic stem cell
8	chr2:186292000-186298200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
9	chr2:186293000-186298200	Weak transcription	HUES64 Cell Line	embryonic stem cell
10	chr2:186293000-186298200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
11	chr2:186293200-186293400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr2:186293200-186295600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr2:186293200-186295600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
14	chr2:186293200-186297600	Weak transcription	HUES6 Cell Line	embryonic stem cell
15	chr2:186293200-186297800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
16	chr2:186293400-186293800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr2:186295600-186295800	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr2:186295600-186296000	Enhancers	iPS-18 Cell Line	embryonic stem cell
19	chr2:186295600-186296200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
20	chr2:186296000-186298200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
21	chr2:186296200-186298200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
22	chr2:186297600-186298600	Enhancers	HUES6 Cell Line	embryonic stem cell
23	chr2:186297800-186298000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
24	chr2:186297800-186298200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr2:186297800-186298400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr2:186297800-186298400	Enhancers	HMEC	breast
27	chr2:186297800-186298600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
28	chr2:186297800-186298600	Enhancers	H9 Cell Line	embryonic stem cell
29	chr2:186297800-186298600	Enhancers	NHEK	skin
30	chr2:186297800-186299200	Enhancers	ES-I3 Cell Line	embryonic stem cell
31	chr2:186297800-186299200	Enhancers	Muscle Satellite Cultured Cells	--
32	chr2:186298000-186298600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr2:186298000-186298800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr2:186298000-186299000	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr2:186298200-186298400	Enhancers	H1 Cell Line	embryonic stem cell
36	chr2:186298200-186298600	Enhancers	iPS-15b Cell Line	embryonic stem cell
37	chr2:186298200-186298600	Enhancers	iPS-20b Cell Line	embryonic stem cell
38	chr2:186298200-186298600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
39	chr2:186298200-186298800	Enhancers	HUES64 Cell Line	embryonic stem cell
40	chr2:186298200-186299000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr2:186298200-186299200	Enhancers	iPS-18 Cell Line	embryonic stem cell
42	chr2:186298200-186315800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr2:186298400-186298600	Flanking Active TSS	HMEC	breast
44	chr2:186298400-186298600	Enhancers	NH-A	brain
45	chr2:186298600-186298800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr2:186298600-186298800	Flanking Active TSS	NHEK	skin
47	chr2:186298600-186299200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
48	chr2:186298600-186299600	Weak transcription	HUES6 Cell Line	embryonic stem cell
49	chr2:186298600-186300400	Active TSS	HMEC	breast
50	chr2:186298600-186315800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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